# | Title | Journal | Year | Citations |
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1 | Toxic equivalency factors (TEFs) for polycyclic aromatic hydrocarbons (PAHs) | Regulatory Toxicology and Pharmacology | 1992 | 2,214 |
2 | Concordance of the Toxicity of Pharmaceuticals in Humans and in Animals | Regulatory Toxicology and Pharmacology | 2000 | 1,602 |
3 | Use of an aggregate exposure model to estimate consumer exposure to fragrance ingredients in personal care and cosmetic products | Regulatory Toxicology and Pharmacology | 2015 | 1,401 |
4 | Novel database for exposure to fragrance ingredients in cosmetics and personal care products | Regulatory Toxicology and Pharmacology | 2015 | 1,343 |
5 | Application of the expanded Creme RIFM consumer exposure model to fragrance ingredients in cosmetic, personal care and air care products | Regulatory Toxicology and Pharmacology | 2017 | 1,342 |
6 | Integrating habits and practices data for soaps, cosmetics and air care products into an existing aggregate exposure model | Regulatory Toxicology and Pharmacology | 2017 | 1,314 |
7 | Correlation of chemical structure with reproductive and developmental toxicity as it relates to the use of the threshold of toxicological concern | Regulatory Toxicology and Pharmacology | 2012 | 1,187 |
8 | A strategy for structuring and reporting a read-across prediction of toxicity | Regulatory Toxicology and Pharmacology | 2015 | 1,125 |
9 | A Systematic Approach for Evaluating the Quality of Experimental Toxicological and Ecotoxicological Data | Regulatory Toxicology and Pharmacology | 1997 | 913 |
10 | Safety Evaluation and Risk Assessment of the Herbicide Roundup and Its Active Ingredient, Glyphosate, for Humans | Regulatory Toxicology and Pharmacology | 2000 | 667 |
11 | Review of health safety aspects of nanotechnologies in food production | Regulatory Toxicology and Pharmacology | 2009 | 647 |
12 | Trace element risk assessment: essentiality vs. toxicity | Regulatory Toxicology and Pharmacology | 2003 | 642 |
13 | Risk assessment of the mycotoxin zearalenone | Regulatory Toxicology and Pharmacology | 1987 | 624 |
14 | Reference dose (RfD): Description and use in health risk assessments | Regulatory Toxicology and Pharmacology | 1988 | 491 |
15 | The safety of chitosan as a pharmaceutical excipient | Regulatory Toxicology and Pharmacology | 2010 | 460 |
16 | Comparison of Cramer classification between Toxtree, the OECD QSAR Toolbox and expert judgment | Regulatory Toxicology and Pharmacology | 2015 | 426 |
17 | Oral toxicity of silver ions, silver nanoparticles and colloidal silver – A review | Regulatory Toxicology and Pharmacology | 2014 | 420 |
18 | The Dermal Sensitisation Threshold—A TTC approach for allergic contact dermatitis | Regulatory Toxicology and Pharmacology | 2008 | 402 |
19 | A rationale for determining, testing, and controlling specific impurities in pharmaceuticals that possess potential for genotoxicity | Regulatory Toxicology and Pharmacology | 2006 | 393 |
20 | Health benefits and potential risks related to consumption of fish or fish oil | Regulatory Toxicology and Pharmacology | 2003 | 390 |
21 | Regulatory history and experimental support of uncertainty (safety) factors | Regulatory Toxicology and Pharmacology | 1983 | 387 |
22 | Risk and safety assessment on the consumption of Licorice root (Glycyrrhiza sp.), its extract and powder as a food ingredient, with emphasis on the pharmacology and toxicology of glycyrrhizin | Regulatory Toxicology and Pharmacology | 2006 | 385 |
23 | Health Implications of Nitrate and Nitrite in Drinking Water: An Update on Methemoglobinemia Occurrence and Reproductive and Developmental Toxicity | Regulatory Toxicology and Pharmacology | 1996 | 384 |
24 | What do we (need to) know about the kinetic properties of nanoparticles in the body? | Regulatory Toxicology and Pharmacology | 2007 | 383 |
25 | Safety and Advantages of Bacillus thuringiensis-Protected Plants to Control Insect Pests | Regulatory Toxicology and Pharmacology | 2000 | 381 |
26 | Extension of the Dermal Sensitisation Threshold (DST) approach to incorporate chemicals classified as reactive | Regulatory Toxicology and Pharmacology | 2015 | 380 |
27 | Bacteriophage P100 for control of Listeria monocytogenes in foods: Genome sequence, bioinformatic analyses, oral toxicity study, and application | Regulatory Toxicology and Pharmacology | 2005 | 375 |
28 | Occurrences, Uses, and Properties of Chromium | Regulatory Toxicology and Pharmacology | 1997 | 373 |
29 | Refinement of the Dermal Sensitisation Threshold (DST) approach using a larger dataset and incorporating mechanistic chemistry domains | Regulatory Toxicology and Pharmacology | 2011 | 371 |
30 | Chromium as an Essential Nutrient for Humans | Regulatory Toxicology and Pharmacology | 1997 | 370 |
31 | Ranking and prioritization of environmental risks of pharmaceuticals in surface waters | Regulatory Toxicology and Pharmacology | 2004 | 362 |
32 | Health safety issues of synthetic food colorants | Regulatory Toxicology and Pharmacology | 2015 | 359 |
33 | Principles for identification of High Potency Category Chemicals for which the Dermal Sensitisation Threshold (DST) approach should not be applied | Regulatory Toxicology and Pharmacology | 2015 | 350 |
34 | Potency Equivalency Factors for Some Polycyclic Aromatic Hydrocarbons and Polycyclic Aromatic Hydrocarbon Derivatives | Regulatory Toxicology and Pharmacology | 1998 | 347 |
35 | Human pharmaceuticals in US surface waters: A human health risk assessment | Regulatory Toxicology and Pharmacology | 2005 | 343 |
36 | Uniform assessment and ranking of opioid Mu receptor binding constants for selected opioid drugs | Regulatory Toxicology and Pharmacology | 2011 | 336 |
37 | Potential adverse effects of phthalic acid esters on human health: A review of recent studies on reproduction | Regulatory Toxicology and Pharmacology | 2008 | 329 |
38 | The hormesis database: The occurrence of hormetic dose responses in the toxicological literature | Regulatory Toxicology and Pharmacology | 2011 | 315 |
39 | IPCS Conceptual Framework for Evaluating a Mode of Action for Chemical Carcinogenesis | Regulatory Toxicology and Pharmacology | 2001 | 313 |
40 | Consumer Exposure to Fragrance Ingredients: Providing Estimates for Safety Evaluation | Regulatory Toxicology and Pharmacology | 2002 | 308 |
41 | Comparative assessment of nanomaterial definitions and safety evaluation considerations | Regulatory Toxicology and Pharmacology | 2015 | 301 |
42 | Assessing skin sensitization hazard in mice and men using non-animal test methods | Regulatory Toxicology and Pharmacology | 2015 | 300 |
43 | Criteria for Development of a Database for Safety Evaluation of Fragrance Ingredients | Regulatory Toxicology and Pharmacology | 2000 | 296 |
44 | Applying Adverse Outcome Pathways (AOPs) to support Integrated Approaches to Testing and Assessment (IATA) | Regulatory Toxicology and Pharmacology | 2014 | 291 |
45 | Regulatory aspects of nanotechnology in the agri/feed/food sector in EU and non-EU countries | Regulatory Toxicology and Pharmacology | 2015 | 291 |
46 | A Cancer Risk Assessment of Di(2-ethylhexyl)phthalate: Application of the New U.S. EPA Risk Assessment Guidelines | Regulatory Toxicology and Pharmacology | 1999 | 290 |
47 | Nanoparticles skin absorption: New aspects for a safety profile evaluation | Regulatory Toxicology and Pharmacology | 2015 | 270 |
48 | Food-processing enzymes from recombinant microorganisms—a review | Regulatory Toxicology and Pharmacology | 2006 | 269 |
49 | A review of the evidence on smoking bans and incidence of heart disease | Regulatory Toxicology and Pharmacology | 2014 | 263 |
50 | Evaluation of the Tobacco Heating System 2.2. Part 2: Chemical composition, genotoxicity, cytotoxicity, and physical properties of the aerosol | Regulatory Toxicology and Pharmacology | 2016 | 256 |